Phenyl 2,3,4,6-Tetra-O-acetyl-α-D-glucopyranoside

≥98%

Reagent Code: #103986
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CAS Number 3427-45-0

science Other reagents with same CAS 3427-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 424.40 g/mol
Formula C₂₀H₂₄O₁₀
badge Registry Numbers
MDL Number MFCD00064090
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

It is commonly used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates. Its acetylated groups make it a valuable building block in carbohydrate chemistry, particularly for creating glycosidic bonds in oligosaccharide synthesis. It is also employed in the preparation of glycosyl donors for glycosylation reactions, which are crucial in the development of glycopeptides, glycolipids, and other bioactive molecules. Additionally, it serves as a precursor in the production of glycosidase inhibitors, which have potential applications in medicinal chemistry and drug development. Its stability and reactivity make it a preferred choice in research focused on glycobiology and the study of carbohydrate-protein interactions.

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Test Parameter Specification
Appearance White Powder or Crystal
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,964.00
inventory 1g
10-20 days ฿17,991.00

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Phenyl 2,3,4,6-Tetra-O-acetyl-α-D-glucopyranoside
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It is commonly used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates. Its acetylated groups make it a valuable building block in carbohydrate chemistry, particularly for creating glycosidic bonds in oligosaccharide synthesis. It is also employed in the preparation of glycosyl donors for glycosylation reactions, which are crucial in the development of glycopeptides, glycolipids, and other bioactive molecules. Additionally, it serves as a precursor in the production of glyco

It is commonly used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates. Its acetylated groups make it a valuable building block in carbohydrate chemistry, particularly for creating glycosidic bonds in oligosaccharide synthesis. It is also employed in the preparation of glycosyl donors for glycosylation reactions, which are crucial in the development of glycopeptides, glycolipids, and other bioactive molecules. Additionally, it serves as a precursor in the production of glycosidase inhibitors, which have potential applications in medicinal chemistry and drug development. Its stability and reactivity make it a preferred choice in research focused on glycobiology and the study of carbohydrate-protein interactions.

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